High-Throughput Screening Identified Compounds Sensitizing Tumor Cells to Glucose Starvation in Culture and VEGF Inhibitors In Vivo.
HTS
cancer metabolism
drug combination
small molecule
synthetic lethality
Journal
Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829
Informations de publication
Date de publication:
30 Jan 2019
30 Jan 2019
Historique:
received:
27
12
2018
revised:
17
01
2019
accepted:
28
01
2019
entrez:
2
2
2019
pubmed:
2
2
2019
medline:
2
2
2019
Statut:
epublish
Résumé
Tumor cells utilize glucose to fuel their anabolic needs, including rapid proliferation. However, due to defective vasculature and increased glucose uptake, tumor cells must overcome glucose deprivation. Accordingly, tumor cells depend on cellular pathways promoting survival under such conditions. Targeting these survival mechanisms can thus serve as a new therapeutic strategy in oncology. As such, we sought to identify small-molecule inhibitors which sensitize tumor cells to glucose starvation by high-throughput drug screening in vitro. Specifically, we searched for inhibitors that selectively killed tumor cells growing in glucose-free but not in normal medium. This phenotypic drug screen of 7000 agents with MCF7 cells led to the identification of 67 potential candidates, 31 of which were validated individually. Among the identified compounds, we found a high number of compounds known to target mitochondria. The efficacies of two of the identified compounds, QNZ (EVP4593) and papaverine, were validated in four different tumor cell lines. We found that these agents inhibited the mTOR(Mechamistic\Mammilian Target of Rapamycin) pathway in tumor cells growing under glucose starvation, but not under normal conditions. The results were validated and confirmed in vivo, with QNZ and papaverine exhibiting superior antitumor activity in a tumor xenograft model when combined with the VEGF inhibitor bevacizumab (avastin). Administering these drug combinations (i.e., avastin and papaverine, and avastin and QNZ) led to significant reductions in proliferation and mTOR activity of the aggressive DLD1 colon cell line in mice. Given our findings, we propose that compounds targeting metabolically challenged tumors, such as inhibitors of mitochondrial activity, be considered as a therapeutic strategy in cancer.
Identifiants
pubmed: 30704052
pii: cancers11020156
doi: 10.3390/cancers11020156
pmc: PMC6406438
pii:
doi:
Types de publication
Journal Article
Langues
eng
Subventions
Organisme : Israel Science Foundation
ID : 221152
Organisme : Israel Science Foundation
ID : 700/16
Organisme : Israeli Cancer Association
ID : 20180012
Organisme : Israeli Cancer Association
ID : 20170024
Références
J Urol. 2002 Feb;167(2 Pt 2):1196
pubmed: 11905900
J Neurosurg. 1992 Dec;77(6):848-52
pubmed: 1432125
Cell. 2003 Nov 26;115(5):577-90
pubmed: 14651849
N Engl J Med. 2004 Jun 3;350(23):2335-42
pubmed: 15175435
Biochem J. 1928;22(5):1289-98
pubmed: 16744142
Cell. 2006 Sep 8;126(5):955-68
pubmed: 16959574
Genes Dev. 2008 Jun 1;22(11):1490-500
pubmed: 18519641
Nat Rev Mol Cell Biol. 2009 May;10(5):307-18
pubmed: 19339977
Cancer Res. 2009 May 15;69(10):4225-34
pubmed: 19435925
Cancer Res. 2009 Jun 1;69(11):4918-25
pubmed: 19458066
Mol Cell. 2010 May 28;38(4):487-99
pubmed: 20513425
Nat Rev Cancer. 2011 Feb;11(2):85-95
pubmed: 21258394
Cell Death Differ. 2012 Mar;19(3):501-10
pubmed: 21941369
Nat Cell Biol. 2011 Aug 28;13(10):1272-9
pubmed: 21968997
Cell. 2012 Apr 27;149(3):656-70
pubmed: 22541435
Nature. 2012 May 09;485(7400):661-5
pubmed: 22660331
Mol Syst Biol. 2012;8:596
pubmed: 22864381
Oncogene. 2014 Feb 6;33(6):745-55
pubmed: 23396361
Cell. 2013 May 23;153(5):1064-79
pubmed: 23706743
Nat Neurosci. 2013 Oct;16(10):1373-82
pubmed: 23995067
Cell Metab. 2013 Nov 5;18(5):726-39
pubmed: 24140020
Oncotarget. 2013 Dec;4(12):2577-90
pubmed: 24342878
Nature. 2014 Apr 3;508(7494):108-12
pubmed: 24670634
Elife. 2014 May 13;3:e02242
pubmed: 24843020
Oncogene. 2015 Jul 23;34(30):4005-10
pubmed: 25284589
Biochim Biophys Acta. 2015 Jul;1849(7):845-60
pubmed: 25464034
Nat Chem Biol. 2015 Jan;11(1):9-15
pubmed: 25517383
Cancer Cell. 2015 Feb 9;27(2):211-22
pubmed: 25620030
Nat Cell Biol. 2015 Apr;17(4):351-9
pubmed: 25774832
Cell. 2015 Jul 16;162(2):259-270
pubmed: 26144316
Cancer Discov. 2015 Oct;5(10):1024-39
pubmed: 26382145
Mol Cell. 2015 Oct 15;60(2):195-207
pubmed: 26474064
PLoS Biol. 2015 Dec 01;13(12):e1002309
pubmed: 26625127
Nat Cell Biol. 2016 Feb;18(2):213-24
pubmed: 26751287
Cell Metab. 2016 Jan 12;23(1):27-47
pubmed: 26771115
Oncogene. 2016 Sep 8;35(36):4675-88
pubmed: 26829052
Cancer Cell. 2016 Apr 11;29(4):548-562
pubmed: 27052953
Neuro Oncol. 2017 Jan;19(1):43-54
pubmed: 27365097
Cell. 2016 Jul 28;166(3):555-566
pubmed: 27471965
Nat Rev Cancer. 2016 Oct;16(10):635-49
pubmed: 27634447
Trends Cancer. 2016 May;2(5):241-251
pubmed: 27668290
Nature. 2017 Feb 2;542(7639):119-123
pubmed: 28099419
Cancer Res. 2017 May 1;77(9):2242-2254
pubmed: 28249898
Cell. 2017 Mar 9;168(6):960-976
pubmed: 28283069
Curr Opin Cell Biol. 2017 Apr;45:102-109
pubmed: 28582681
Nat Med. 2017 Nov;23(11):1342-1351
pubmed: 29035366
Mol Cell. 2017 Dec 7;68(5):885-900.e6
pubmed: 29220654
Cancer Cell. 2017 Dec 11;32(6):807-823.e12
pubmed: 29232555
Medchemcomm. 2017 Feb 20;8(3):657-661
pubmed: 30108783
Proc Natl Acad Sci U S A. 2018 Oct 16;115(42):10756-10761
pubmed: 30201710
J Neurochem. 1996 Mar;66(3):1174-81
pubmed: 8769881